The CCN family member Wisp3, mutant in progressive pseudorheumatoid dysplasia, modulates BMP and Wnt signaling

Author:

Nakamura Yukio,Weidinger Gilbert,Liang Jennifer O.,Aquilina-Beck Allisan,Tamai Keiko,Moon Randall T.,Warman Matthew L.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference68 articles.

1. Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia

2. Sewairi, W., and Warman, M.L. 2003. Wisp3 and progressive pseudorheumatoid dysplasia. InMolecular basis of inborn errors of development. C.J. Epstein, A. Wynshaw-Boris, and R.P. Erickson, editors. Oxford University Press. Oxford, United Kingdom. 282–284.

3. Progressive pseudorheumatoid arthropathy of childhood (PPAC): A hereditary disorder simulating juvenile rheumatoid arthritis

4. Spondylo-epiphysial dysplasia tarda with progressive arthropathy. A "new" disorder of autosomal recessive inheritance

5. Progressive pseudorheumatoid dysplasia: report of a family and review.

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